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Shade-Dwelling Corals of the Great Barrier Reef

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Shade-Dwelling Corals of the Great Barrier Reef SERIES Vol. 10: 173-185, 1983 MARINE ECOLOGY - PROGRESS Published January 3 Mar. Ecol. Prog. Ser. Shade-Dwelling Corals of the Great Barrier Reef Zena D. Dinesen* Department of Marine Biology, James Cook University. Townsville, Queensland 481 1, Australia ABSTRACT: Shade-dwelling corals were studied from 127 caves, tunnels, and overhangs from a variety of reefs within the Great Barrier Reef Province. Over 3,000 coral colonies were recorded from these shaded habitats, and more than 150 species, mostly herrnatypic, were represented. Three groups of shade-dwelling corals are tentatively distinguished: generally skiophilous (shade-loving) corals, found both in deep water and in shallow but shaded conditions; preferentially cavernicolous corals, growing mostly in shallow, shaded habitats; and shade-tolerant corals, common also in better illumi- nated parts of the reef, but tolerant of a wide range of conditions. Hermatypic shade-dwelling corals usually have thin, flattened growth forms, and the coralla are generally small, suggesting that low light intensity is restricting both the shape and size of colonies. Apart from an abundance of ahermatypic corals on the ceilings of some cavities, particular fauna1 zones were not detected in different sectors of cavities or at different irradiance levels. This lack of zonation is attributed principally to 2 factors. Firstly, the coral fauna represents only a well shaded but not 'obscure' (dark) aspect of skiophilous communities; secondly, ahermatyplc corals were not found in conditions darker than those tolerated by some hermatypic species. INTRODUCTION nicolous and bathyal sponge faunas have been noted at Madagascar (Vacelet and Vasseur, 1977). The Recent workers (Hartman and Goreau, 1970; Jack- emergence of various sponges (including sclero- son et al., 1971; Jaubert and Vasseur, 1974; Bonem, sponges) and brachiopods from shaded habitats with 1977; Vasseur, 1977) have emphasized the signifi- increasing depth has also been observed (Hartman, cance, within the coral reef framework, of shaded envi- 1973, 1977; Noble et al., 1976; Logan, 1977). However, ronments which offer skiophilous organisms an impor- the cave-dwelling fauna is not only representative of a tant refuge from competition with faster growing deep water fauna displaced into shallow, shaded envi- species of the 'open' reef. Shaded habitats may contain ronments. For example, Vasseur (1974) has reported a wide range of sessile cryptic organisms, including that some pharetronid sponges are strictly caver- sponges, algae, coelenterates, brachiopods, bryozoans, nicolous. serpulid worms, encrusting foraminiferans, ascidians, Despite the increasing attention being focused on and bivalve molluscs (Laborel, 1960; Per& and Picard, shaded reef habitats, little information has been col- 1964; Vacelet, 1967a, b; Hartman and Goreau, 1970; lected on the cave-dwelling scleractinian fauna of Jackson et al., 1971; Pouliquen, 1971; Vasseur, 1974, Indo-Pacific reefs. The only detailed records are from 1977; Bonem, 1977; Cuffey and Fonda, 1977; Logan, the southwest Indian Ocean (Jaubert and Vasseur, 1977). These organisms are distributed primarily 1974; Vasseur, 1974, 1977). according to irradiance levels, although water move- From Madagascar, Jaubert and Vasseur (1974) ment may also influence their distribution. described skiophilous communities from a wide range Some components of shallow, cryptic communities of shaded and dark reef cavities. Three basic commun- also occur in deep water. For instance, bathyal sponges ity types have been defined, according to irradiance have been found in dark caves in the Mediterranean levels, and sometimes hydrodynamic factors (Vasseur, Sea (Pouliquen, 1969), and similarities between caver- 1974). Hermatypic corals, occurring at 2.0 to 8.0 % subsurface irradiance, are characteristic of a better illuminated aspect dominated by algae. Ahermatypic Present address: Australian Institute of Marine Science, species are notable in some shaded 'animal-dominant' P.M.B.No. 3, M.S.O.Townsville, Queensland 4810, Australia facies. Species of Dendrophyllia and Tubastraea are O Inter-Research/Printed in F. R. Germany 174 Mar. Ecol. Prog. Ser found at 0.5 to 4.0 % subsurface irradiance (often ceiling, back wall, floor, and 2 side walls. The position > 1.0 %), while other ahermatypes (species of Phyllan- of a colony on one of these surfaces was further defined gia, Culicia, and Balanophyllia) occur at slightly lower with respect to its proximity to the aperture. Although irradiance levels (< 0.1 % subsurface light).The cavity shape did not always conform to the theoretical 'exclusively animal' biocoenosis, confined to darker cube, the data indicate possible preferences of species conditions, is characterized by sponges, and is appa- for growing on certain cavity surfaces. rently devoid of corals. As part of a research programme on coral distribu- tion patterns, the author has investigated shade-dwell- ing scleractinians of the Great Barrier Reef (G.B.R.). This study revealed definite regional differences in the shade-dwelling coral fauna, with cavities in the south- em part of the G.B.R. tending to have an impoverished coral fauna compared with that recorded further north. These regional variations are discussed elsewhere (Dinesen, 1982). This paper investigates the nature of the shade-dwelling coral fauna, to determine whether it is basically cavernicolous, or if it has closer affinities with assemblages from deep water, or from shallow, 'open' reef areas. The distribution and zonation of coral species within cavities and according to irradiance levels are examined, and modifications of growth form and other adaptive strategies of shade-dwelling corals, are discussed. METHODS Field Methods Sampling localities represent a wide range of reef types from various sectors of the G.B.R. In the Lizard Island region (14'-15" S; Fig. l),100 reef cavities were investigated. Study sites included the fringing reefs and lagoon of the Lizard Island Group; outer slope, reef channel, and back reef areas of 5 outer barrier reefs (Jewell, Carter, Yonge, No Name, and South Ribbon Fig. 1. Reefs in Lizard Island region. Sampling localities Reefs); and North Direction Island, Eyrie, and MacGil- given in text. Inset of Queensland coast indicates general livray Reefs. Two cavities were studied at Keeper Reef locations of study areas (18'45' S, 147" 15' E), and a further 25 at Heron, Wis- tari, and Wilson Reefs in the Capricorn Group (around ONORTH REEF 23' S; Fig. 2). All cavities investigated were within the ISLIND TRYON ISLAND reef slope in a depth range of 4 to 21 m (approximately .o O~ZE~TFIELD D OWILSOII 1SLI.D below low water datum). NORTH WEST lSLAND %RECI ISLAND i CAPRICORN For every coral in each cavity were recorded its GROUP WIST~RIREEF OSVKES REEF identity, colony size and shape, position within the 'lPECApRIEORN ERSKINE ISLAND 0 Q 23°30'S- cavity, and the irradiance level at which it occurred. MASTHEAD ISLAND ONE TREE ISLAND c,-- Colony size was determined from maximum length POLMllSE REEF LAMONT REEF 4 QFITZROI REEF and maximum width perpendicular to the length (mea- r-\/ LLEWELLYN REEF sured to the nearest cm). Since most colonies were . (7 BOULT REEFO rather flat, measurements in 2 dimensions were consi- BUNKER GROUP HOSKYN ISLANDS@ dered adequate. The overall growth form was FAIRFAX ISLANDSO recorded, and any remarkable growth modifications MUSORAVE ISl!:iJ@ noted. 1 S Z00O'E To expedite recording the locations of coral colonies, Fig. 2. Reefs in Capricorn region. Sampling localities given in each cavity was treated as a theoretical cube, with text Dinesen: Shade-dwelling corals of Great Barrier Reef 175 Irradiance readings were taken with a Gossen applied to test whether these species occurred more Lunasix-3 lightmeter. Similar equipment has been often, or less frequently, at cavity apertures. used in studies of coral calcification and photosynthe- Multiple range tests were used to compare mean tic carbon fixation (Barnes and Taylor, 1973). The irradiance records for shade-dwelling coral species, range of sensitivity is 0.17 to 350,000 lux (1 Klux = and mean values for maximum colony length, and 19.5 ~Einsteinsm-'S-' = 4.27 watts m-', surface solar maximum colony area. The test used was Modified irradiance [400 to 700 nm]). The equipment is Least Significant Difference, a test exact for unequal designed so that once a reading is taken, the meter can group sizes, available with the SPSS package (Nie et be turned off, but the reading is retained on the scale. al., 1975). To investigate the relationship, if any, Thus records could be taken with the meter held at between colony size and irradiance, simple regres- arm's length to reduce the effect of shadow caused by sions were carried out (again using SPSS) for both the observer. Some cavities were too small for a diver maximum colony length and maximum colony area to enter to obtain incident light measurements, thus with irradiance records. measurements were restricted to reflected light (less Analyses were performed only for the more fre- than the amount of incident light). Light readings quently encountered corals, i. e. those with 15 or more taken for individual corals were expressed as a percen- records. Data for distribution on cavity surfaces, tage of the mean subsurface irradiance falling on a irradiance levels, colony size, and growth forms of horizontal plane (the mean calculated from readings hermatypes, are presented only for these more com- taken before and after the
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